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Compounded versions of tirzepatide (Mounjaro, Zepbound) containing vitamin B12 pose a potential safety risk to the public, Eli Lilly warned in an open letter on Thursday. Following laboratory testing, the drugmaker said
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The FDA has sent 30 warning letters to telehealth companies for falsely marketing compounded GLP-1s, which are not FDA-approved and can pose risks to patients. FULL STORY:🔗https://tinyurl.com/3ztf9uj2
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The FDA has issued warning letters to multiple companies marketing compounded Retatrutide, an investigational drug from Eli Lilly still in Phase II trials. While early studies have shown promising weight-loss results, Retatrutide
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Have patients been harmed by unsafe drug compounding? – Partnership for Safe Medicines
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The New York Times spotlighted MEDVi. The FDA had already warned the self-proclaimed 'fastest growing company in history.'
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Report: FDA must enforce rules on compounded GLP-1s
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Beyond the Headlines: FDA Warning Letters to GLP-1 Compounders
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